Susana avila martinez purpura trombocitopenica trombotica 2. Purpura results from the extravasation of blood cells into the skin andor mucous membranes giving rise to small purple coloured areas that do not disappear under pressure. Thrombotic thrombocytopenic purpura, atypical hemolytic uremic syndrome. Feb 08, 2016 purpura trombocitopenica trombotica 1. Thrombocytopenia during pregnancy is associated with many diseases, of which idiopathic thrombocytopenic purpura is the most common in the first trimester. Approach to the investigation and management of immune thrombocytopenic purpura in children. Idiopathic thrombocytopenic purpura is an autoimmune disorder characterized by a low platelet count. He proposed that a powerful poison with both agglutina. Thrombocytopenia during pregnancy is associated with many diseases, of which idiopathic thrombocytopenic purpura. Assessment of uk practice for management of acute childhood idiopathic thrombocytopenic purpura against. Autoimmmune thrombocytopenic purpura atp is a hemorrhagic disease. Purpura trombocitopenica e anemia hemolitica autoimune em pacientes. Pdf trombocytopenic purpura and autoimmune hemolytic anemia.
Sequential occurrence of thrombotic thrombocytopenic purpura, essential thrombocythemia, and idiopathic thrombocytopenic purpura in a 42yearold africanamerican woman. Epistaxis gingivorragia melenas hematuria con poca frecuencia. Primary immune thrombocytopenia itp is an acquired immunemediated disorder characterized by isolated low platelet count and the absence of any other cause of the thrombocytopenia. Thrombocytopenic purpura is mostly responsible for episodes of mucocutaneous bleeding. Purpura trombotica trombocitopenica ptt the oncology. Esta enfermedad afecta a varones y a mujeres por igual.
Autoimmmune thrombocytopenic purpura atp is a hemorrhagic disease with a more frequent presentation in infancy. Primary immune thrombocytopenia, formerly known as immune thrombocytopenic purpura, is a disease for which the clinical and therapeutic management has always been controversial. The entire sample 200 patients had idiopathic thrombocyto penic purpura. The etiopathogenic mechanisms may result from abnormalities in any of the three components of hemostasis. Purpura trombocitopenico inmune idiopatico slideshare. Chronic immune thrombocytopenic purpura itp is a bleeding disorder characterized by increased destruction of platelets due to the production of antiplatelet autoantibodies. Trombocitopenia inmune care guide information en espanol. It can produced in health people, but in children has been associated to viral infection, or bacterial infection. Purpura trombocitopenica autoinmune caso clinico y revision bibliografica luis angel sequeira rojas s u m m a r y the itp is a blood illness, characterize by thrombocytopenic, and it variability intense level.
Purpura trombocitopenica imune gratis artigos academicos. Thrombotic thrombocytopenic purpura description of diagnosis and management of a rare entity with a high mortality. Grading of hemorrhage in children with idiopathic thrombocytopenic purpura. Thrombotic thrombocitopenic purpura is a rare disease with a morphological expression featured of many microthrombi in the terminal arterioles of several vital structures.
Could appear with an all level of bleeding and sometimes involves the central nervous system cns. Purpura trombotica trombocitopenica y sindrome hemolitico uremico. Rituximab en purpura trombocitopenica inmune refractaria. Purpura trombocitopenica by iveett soriano on prezi. Purpura are injuries caused by the extravasation of blood cells into the skin and or mucous membranes due to hemostasis disorders. Trombocitopenia inmune persistente y cronica del adulto revista. Eperto e bases del diagstico e hematologa 4 purpura trombotica trombocitopenica y sindrome hemolitico uremico figura 1. Purpura trombocitopenica inmune cronica y recurrente sciencedirect. Purpura trombocitopenica inmune idiopatica en ninos. Onset usually occurs during adolescence with episodes of cutaneous and mucosal bleeding. Moschcowitz was the first to inform multiple hyaline thrombi as the primordial finding of a partial autopsy case. Purpura trombocitopenica autoinmune caso clinico y. Adamts, purpura trombotica trombocitopenica, sindrome uremico hemolitico atipico.
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